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Journals Case Reports in Oncological Me...

Case Reports in Oncological Medicine

https://read.qxmd.com/read/36394062/development-of-merkel-cell-carcinoma-in-a-patient-receiving-rituximab
#21
Bana Antonios, Ujjwal Karki, Kais Antonios, Bipin Ghimire, Mohammad Muhsin Chisti
Merkel cell carcinoma (MCC) is a rare, rapidly growing, and aggressive dermatological neoplasm. It is commonly reported in Caucasian ethnicities, and almost 50% of the patients have a concomitant malignancy and are on immunosuppressive chemotherapy. Here, we present a 79-year-old woman with a history of relapsed Stage II, grade III follicular lymphoma, receiving maintenance rituximab infusions. She presented with a raised erythematous papule on her left cheek. An excisional biopsy of the lesion confirmed a diagnosis of Merkel cell carcinoma...
2022: Case Reports in Oncological Medicine
https://read.qxmd.com/read/36329810/acute-adrenal-hemorrhage-as-the-initial-manifestation-of-metastatic-lung-adenocarcinoma-a-cautionary-tale
#22
Sowbharnika Arivazhagan, Guru Prasad Parthiban, Christina Patterson, Karthik Reddy
Adrenal gland metastatic disease is the most commonly occurring malignancy of the adrenal glands. Although metastatic disease is common, adrenal hemorrhage is a rare but potentially fatal manifestation of malignancy. The objectives of this case report are to highlight the unusual presentation of metastatic lung adenocarcinoma as spontaneous adrenal hemorrhage in a 64-year-old female who was otherwise asymptomatic. As well as to support the reasoning that metastatic disease should be considered as a differential in patients with this clinical presentation as this may have altered this fatal outcome...
2022: Case Reports in Oncological Medicine
https://read.qxmd.com/read/35685062/surgical-treatment-of-single-pontomedullary-junction-metastasis-from-lung-cancer
#23
Paolo Missori, Simone Peschillo, Angela Ambrosone, Antonio Currà, Sergio Paolini
Background: When lung cancer develops a solitary metastasis at the pontomedullary junction, due to surgical risk, the current oncologic treatment is radiosurgery and chemotherapy. Case Description . We describe a patient with a single intrinsic metastasis at the pons and medulla. Removal was successful, without complication. Conclusion: Surgery can provide excellent results, and in selected patients, it should be considered a first-line treatment in experienced hands...
2022: Case Reports in Oncological Medicine
https://read.qxmd.com/read/35685061/primary-eccrine-porocarcinoma-of-the-breast-a-case-report-and-review-of-literature
#24
Yi Xin Li, Mihir Gudi, Zhiyan Yan
Eccrine porocarcinoma (EPC) is a rare cutaneous neoplasm, with less than 500 reported cases worldwide since it was first described in 1963. EPC tends to affect the elderly and most commonly affects the head and neck. The mainstay of EPC treatment is surgery, with lymphadenectomy in the case of nodal involvement or presence of unfavourable characteristics. No evidence exists to guide the use of adjuvant chemotherapy or radiation. EPC is prone to misdiagnosis given its multiple clinical and histopathological mimics, especially in uncommon sites of presentation such as the breast...
2022: Case Reports in Oncological Medicine
https://read.qxmd.com/read/35685060/a-south-african-breast-implant-associated-anaplastic-large-cell-lymphoma-clinical-presentation-and-six-year-follow-up
#25
Alexandra Grubnik, Yastira Ramdas, Barend Van der Bergh, Simon Nayler, Carol-Ann Benn, Bernardo L Rapoport
Breast augmentation is the most common surgical procedure for women globally, with 1,795,551 cases performed in 2019. Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) is highly uncommon, with 733 reported cases as of January 2020. In South Africa, there are less than 4000 breast augmentation surgeries annually. This case presents the first case report documentation of a South African woman diagnosed with BIA-ALCL. The patient was a 61-year-old woman who consulted the Breast Care Centre of Excellence in Johannesburg in 2015...
2022: Case Reports in Oncological Medicine
https://read.qxmd.com/read/35637677/a-rare-case-of-pure-primary-large-cell-neuroendocrine-carcinoma-of-the-gallbladder
#26
Rodney E Shackelford, Ekin Ozluk, Jehan Abdulsattar, Terry C Lairmore, Quyen Chu, Eric X Wei
Primary large cell neuroendocrine carcinoma (LCNEC) of the gallbladder is a rare malignancy which is often associated with non-LCNEC histologic components. Histologically "pure" LCNECs of the gallbladder are exceedingly rare with only 15 cases reported in the medical literature. Clinically, LCNECs present with abdominal pain and jaundice and follow an aggressive course with patients surviving a median of 15 months following initial diagnosis. To our knowledge, we present the 16th case of a histologically pure LCNEC in a 62-year-old African American male who was successfully treated surgically...
2022: Case Reports in Oncological Medicine
https://read.qxmd.com/read/35535354/eosinophilic-asthma-secondary-to-adjuvant-anti-pd-1-immune-checkpoint-inhibitor-treatment-in-a-melanoma-patient
#27
P Kissoonsingh, B Sutton, Syed U Iqbal, Lalit Pallan, Neil Steven, L Khoja
Background: Adjuvant immune checkpoint inhibitors are a new standard of care in melanoma. However, the immune related toxicity associated with these agents can be serious, and the long-term implications are yet to be defined especially in the adjuvant setting. We report, to our knowledge, the first case of anti-PD-1-induced eosinophilic asthma in a melanoma patient treated with adjuvant pembrolizumab. Case Presentation. A 72-year-old man commenced pembrolizumab in the adjuvant setting after resection of a stage IIIB cutaneous melanoma...
2022: Case Reports in Oncological Medicine
https://read.qxmd.com/read/35469272/a-pulmonary-zebra-adult-primary-pulmonary-synovial-sarcoma
#28
Sheffield Sandra, Nwachukwu Chidi, Ashby Tracy
Primary pulmonary synovial sarcoma (PPSS) is an extremely rare tumor, with approximately 50 cases being reported in the English literature (Golota et al., 2018). Difficulties are often encountered in the diagnosis of PPSS as it can be confused with other spindle or round cell tumors, such as fibrosarcoma, hemangiopericytoma, mesothelioma, sarcomatoid carcinoma, or metastatic sarcomas. PPSS was first described by Zeren et al. in 1995. We present a case of PPSS in a 41-year-old woman, who complained of progressive dyspnea and left-sided chest pain...
2022: Case Reports in Oncological Medicine
https://read.qxmd.com/read/35251725/a-rare-case-of-large-vessel-vasculitis-following-checkpoint-inhibitor-therapy-and-pegfilgrastim
#29
Joseph Mort, Shipra Maheshwari, Nayanika Basu, Patrick Dillon, Kevin Brady, Harry Bear, Trish Millard
Checkpoint inhibitors (CPIs) and pegfilgrastim, a long-acting growth factor agent, are vital components of current cancer treatments. Immune-related adverse events (irAEs) such as colitis and pneumonitis are well-established toxicities associated with CPI therapy. However, large-vessel vasculitis secondary to CPI utilization is reported only in rare case reports and case series. Interestingly, large-vessel vasculitis has also been reported as a rare complication of pegfilgrastim use. We present a 59-year-old female with left stage IIA (cT2N0M0) triple-negative breast cancer receiving neoadjuvant decitabine and pembrolizumab prior to neoadjuvant chemotherapy (NAC)...
2022: Case Reports in Oncological Medicine
https://read.qxmd.com/read/35127188/atezolizumab-induced-sarcoidosis-like-reaction-in-a-patient-with-metastatic-breast-cancer
#30
Akira Tsunoda, Toshiro Mizuno, Shohei Iida, Katsunori Uchida, Masako Yamashita, Koshi Sukeno, Hiroki Oka, Yasutaka Tono, Mikiya Ishihara, Kanako Saito, Satoshi Tamaru, Keiichi Yamanaka, Isao Tawara
Tumor-related sarcoidosis-like reactions (SLR) have been reported with the use of immune checkpoint inhibitors (ICIs). We report a case of 50-year-old woman who observed an enlarged lymph node in the right hilar region and the appearance of a subcutaneous mass in the extremities during chemotherapy with atezolizumab plus nab-paclitaxel for metastatic triple-negative breast cancer (TNBC). Skin biopsy revealed the formation of epithelioid granulation species with the Langhans giant cell. After discontinuing atezolizumab in the treatment procedure, the hilar lymph nodes and the subcutaneous mass were reduced...
2022: Case Reports in Oncological Medicine
https://read.qxmd.com/read/34900355/late-lung-metastasis-in-a-patient-with-a-clear-cell-chondrosarcoma-an-indication-for-a-life-long-follow-up
#31
Paulien West, Celine Jacobs, Michael Saerens, David Creytens, Gwen Sys, Lore Lapeire
Background: Clear cell chondrosarcoma (CCCS) is a rare subtype of chondrosarcoma and comprises between 1.6% and 2.5% of all chondrosarcoma. They are known to be chemo- and radiotherapy resistant; surgical resection is therefore the therapy of choice. Methods: We present a 63-year-old woman with a progressive lung nodule 20 years after initial diagnosis and treatment of a clear cell chondrosarcoma of the right os naviculare. Results: On serial CT scans of the chest, an asymptomatic, slowly growing nodule in the left upper lung lobe was detected...
2021: Case Reports in Oncological Medicine
https://read.qxmd.com/read/34877023/primary-intraosseous-synovial-sarcoma-in-the-mandible
#32
Lucas Novaes Teixeira, Eduardo Zambaldi da Cruz, Ana Cláudia Garcia Rosa, Anderson Abdo Rodrigues, Fabrício Passador-Santos, Vera Cavalcanti de Araújo, Andresa Borges Soares
Synovial sarcoma (SS) is a rare malignant mesenchymal tumor that mainly occurs in body extremities, being uncommon in the head and neck region. In the present study, we described a case of primary intraosseous SS arising in the mandible of a 22-year-old young male. The patient reported a painful swelling on the left side of the mandible for the last 7 months. Imaging exams showed the presence of an expansive and multilocular radiolucent lesion, extending from the left condyle to the mandibular body. The clinic diagnostic hypotheses were ameloblastoma or malignant neoplasm...
2021: Case Reports in Oncological Medicine
https://read.qxmd.com/read/34868692/pericardial-relapse-of-acute-lymphoblastic-leukemia-all
#33
Diana V Maslov, Ambuga Badari
Acute lymphoblastic leukemia (ALL) is a neoplasm of the B cell or T cell. Diagnosis is made by peripheral blood smear and bone marrow biopsy. Those with relapse/measurable residual disease (MRD) present with fever, weakness, fatigue, and easy bruising due to bone marrow infiltration (Kantarjian et al., 2017). A 59-year-old male with history of relapsed acute lymphoblastic leukemia and allogeneic stem cell transplant presented to the Emergency Department (ED) multiple times with shortness of breath. 2D Echo revealed recurrent pericardial effusion...
2021: Case Reports in Oncological Medicine
https://read.qxmd.com/read/34845431/recurrent-solitary-fibrous-tumor-in-intradural-extramedullary-space-case-report-and-review-of-the-literature
#34
Neris Dincer, Melisa Bagci, Metin Figen, Adem Yilmaz, Ahmet Mesrur Halefoglu, Canan Tanik, Esengul Kocak Uzel
Solitary fibrous tumor/hemangiopericytoma (SFT/HPC) is a rare neoplasm arising from spindle cells and most commonly arising from pleura. Spinal SFT/HPC is a rare entity; hence, it is not on the top of the differential diagnosis list when a clinician faces a spinal lesion. In the review of the literature, there exist less than 50 case reports of intradural extramedullary SFT/HPC. Here, we present a 54-year-old female patient who underwent subtotal surgical excision of an intradural extramedullary spinal mass pathologically reported to be SFT/HPC and had symptomatic recurrence in the 3rd year of follow-up...
2021: Case Reports in Oncological Medicine
https://read.qxmd.com/read/34754521/an-atypical-presentation-of-sinonasal-tract-alveolar-rhabdomyosarcoma-in-a-young-male-patient-submitted-to-multimodality-treatment
#35
Wilber E Bernaola-Paredes, Sergio Leonardo Favareto, Valdener Bella Filho, Eloah Pascuotte Filippetti, Walkiria Pantoja Bellotto, Henrique Rocha Mazorchi Veronese, Lucas Neves de Martins Moraes, Felipe D'Almeida Costa, Antonio Cassio Assis Pellizzon
Rhabdomyosarcoma (RMS), a malignant tumor derived from the neoplastic proliferation of striated skeletal muscle cells, is the most common pediatric soft tissue sarcoma. Its treatment is mainly based on neoadjuvant chemotherapy (QT+), surgical resection, and adjuvant radiotherapy (RT+). RT+ has shown satisfactory results for locoregional control of the disease, in spite of promoting local side effects. The present case report was aimed at describing the clinical and therapeutic characteristics and the management of complications resulting from multimodal therapy in a patient with an atypical presentation of RMS in the sinonasal tract...
2021: Case Reports in Oncological Medicine
https://read.qxmd.com/read/34721913/radiation-recall-dermatitis-following-radioactive-iodine-therapy-a-new-observation
#36
Ikechukwu Chidobem, Tahereh Orouji Jokar, Chisom Mgbodile, Francis Mgbodile, Ghassan Bassil, Nazia Khan
A 47-year-old female, who had previously received adjuvant right breast radiation for ductal carcinoma in situ, presented with right breast edema, erythema, and pain. This developed about two and a half weeks following radioactive iodine therapy for thyroid carcinoma. A biopsy was performed to rule out malignancy, since inflammatory breast cancer can present with similar symptoms. This confirmed radiation recall dermatitis (RRD) as the most likely diagnosis. RRD is an inflammatory reaction occurring in a previously irradiated field and was first described in 1959...
2021: Case Reports in Oncological Medicine
https://read.qxmd.com/read/34671494/salivary-duct-carcinoma-case-reports-and-brief-review-of-the-literature
#37
Deepti Kantamani, Sai S Bandaru, Jennifer L Miatech, M Patrick Stagg
Salivary duct carcinoma (SDC) is an uncommon and highly aggressive tumor associated with high morbidity and mortality. According to the World Health Organization, it is an extremely rare malignancy with an estimated incidence of 1-1.2 in 1,000,000 patients. Standard treatment for SDC is wide surgical resection along with lymph node dissection followed by adjuvant radiation therapy. The role of adjuvant chemotherapy is not known. In this report, we present three cases of SDC. A 71-year-old female with T1N0M0 disease was treated with total parotidectomy, ipsilateral neck dissection, and adjuvant radiotherapy without evidence of disease recurrence at 5 months...
2021: Case Reports in Oncological Medicine
https://read.qxmd.com/read/34659849/thoracodorsal-artery-perforator-flap-for-chronic-radiation-induced-ulcer-of-the-axilla-in-vietnam
#38
Hong Quang Le, Anh Dung Hoang
Breast cancer is the leading cause of death in females worldwide. Radiotherapy plays an important role for locoregional control in the comprehensive management of breast cancer. Chronic radiation-induced ulcer of the axilla can occur, and it is complicated to treat for these lesions. The application of a thoracodorsal artery perforator flap offers many advantages to be one of the most efficient treatments for radiation-induced ulcers of the axillary region. We introduce a series of 5 patients with radiation-induced ulcers of the axilla treated by using a thoracodorsal artery perforator flap...
2021: Case Reports in Oncological Medicine
https://read.qxmd.com/read/34567815/sporadic-burkitt-lymphoma-presenting-with-middle-cranial-fossa-masses-with-sphenoid-bony-invasion-and-acute-pancreatitis-in-a-child
#39
Tal Dror, Virginia Donovan, Naomi Strubel, Sucharita Bhaumik
Acute pancreatitis in children is usually due to infection, trauma, or anatomical abnormalities and is rarely due to obstruction from malignancy. Sporadic Burkitt lymphoma (BL) is an aggressive non-Hodgkin B-cell lymphoma that usually involves the bowel or pelvis, with isolated cases presenting as acute pancreatitis. We report a case of BL in a 12-year-old male presenting as acute pancreatitis with obstructive jaundice and a right middle cranial fossa mass invading the sphenoid bone. The common bile duct in this case was dilated to 21 mm in diameter on abdominal ultrasound and to 26 mm on magnetic resonance cholangiopancreatography (MRCP), significantly greater than any value reported in the literature for BL...
2021: Case Reports in Oncological Medicine
https://read.qxmd.com/read/34395004/pancreatic-neuroendocrine-tumor-with-benign-serous-cystadenoma-a-rare-entity
#40
Randhir Sagar Yadav, Ashik Pokharel, Shumneva Shrestha, Ashbita Pokharel, Deepshikha Gaire, Sumita Pradhan, Prasan Bir Singh Kansakar
Mixed serous-neuroendocrine neoplasm constitutes pancreatic serous cystic neoplasms and pancreatic neuroendocrine tumor, two tumor components with different underlying pathologies. The differentiation of these tumors is important as the management and prognosis depend on the pancreatic neuroendocrine tumor component. We report a case of mixed serous-neuroendocrine neoplasm in a 47-year-old female who presented with epigastric pain abdomen for two years. Imaging studies, tumor markers, thorough systemic evaluation, surgical resection, histopathological examination, and timely follow-up constituted our management approach...
2021: Case Reports in Oncological Medicine
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